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nis-elements real-time deconvolution two-dimensional software  (Nikon)


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    Nikon nis-elements real-time deconvolution two-dimensional software
    Nis Elements Real Time Deconvolution Two Dimensional Software, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/two-dimensional+deconvolution/pm22374978-97-20-27
    Average 90 stars, based on 1 article reviews
    nis-elements real-time deconvolution two-dimensional software - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Absence of the axon initial segment in sensory neuron enhances resistance to amyotrophic lateral sclerosis.
    Article Snippet: 3D reconstructions of the images were generated using NIS-Elements software (Nikon).

    Article Title: Irradiation of prostate cancer alters circulating small extracellular vesicle functions.
    Article Snippet: All colonies were counted and classified by size via the NIS-Elements-F software and Nikon Eclipse TS100 microscope at 40x magnification for PC3 cells or for DU145 cells; 10–12 random optical fields were counted per experimental condition.

    Article Title: Effects of in ovo stimulation with potential epigenetic modulators on immune system phenotype across three generations in a chicken model.
    Article Snippet: These measurements were obtained from microphotographs taken at 40× or 100× magnification using NIS-Elements BR 5.41 imaging software (Nikon).

    Article Title: Renal ischemia/reperfusion injury triggers proximal tubular apoptosis and NHE3 dysfunction via p38MAPK/ezrin signaling pathway.
    Article Snippet: The fluorescence signal was examined using a Nikon Eclipse 80i microscope equipped 622 with a 40x objective and NIS-Elements Basic Research software.

    Article Title: Nuclear morphometrics coupled with machine learning identifies dynamic states of senescence across age.
    Article Snippet: Cryosections were generated on a Leica cryostat at a thickness of 12 μm, allowed to dry for 30min, and stored at −80 °C.

    Article Title: Renal ischemia/reperfusion injury triggers proximal tubular apoptosis and NHE3 dysfunction via p38MAPK/ezrin signaling pathway.
    Article Snippet: Images were examined with an Eclipse 80i 606 microscope (Nikon, Tokyo, Japan) equipped with a 40x objective and NIS-Elements Basic Research 607 software (Nikon).

    Microscopy:

    Article Title: Preventing vision loss in a mouse model of Leber Congenital Amaurosis by engineered tRNA
    Article Snippet: .. The flattened RPE layer was mounted on a cover glass and imaged with NIS-Elements using a Nikon C2 confocal microscope (Nikon Instruments Inc.). ..

    Article Title: Confrontations of the Pathogenic Fungus Colletotrichum graminicola With a Biocontrol Bacterium or a Ubiquitous Fungus Trigger Synthesis of Secondary Metabolites With Lead Structures of Synthetic Fungicides.
    Article Snippet: Differential interference contrast (DIC) and fluorescence microscopy were performed using a Nikon Eclipse 600 microscope (Nikon, Düsseldorf, Germany). .. Digital images were taken with a Nikon microscope camera DS- Ri2, and image processing was performed with NIS- Elements imaging software (Nikon, Düsseldorf, Germany). .. For straining of fungal cell walls, Calcofluor White- M2R (CFW; Sigma- Aldrich, Steinheim, Germany) was mixed with 10% (w/v) KOH at a ratio of 1:1, applied to the sample, and incubated for 15 min at room temperature before inspection by fluorescence microscopy at 350 nm and 25% laser light transmission (Nikon Eclipse 600, UV- 2A filter, Düsseldorf, Germany).

    Imaging:

    Article Title: Confrontations of the Pathogenic Fungus Colletotrichum graminicola With a Biocontrol Bacterium or a Ubiquitous Fungus Trigger Synthesis of Secondary Metabolites With Lead Structures of Synthetic Fungicides.
    Article Snippet: Differential interference contrast (DIC) and fluorescence microscopy were performed using a Nikon Eclipse 600 microscope (Nikon, Düsseldorf, Germany). .. Digital images were taken with a Nikon microscope camera DS- Ri2, and image processing was performed with NIS- Elements imaging software (Nikon, Düsseldorf, Germany). .. For straining of fungal cell walls, Calcofluor White- M2R (CFW; Sigma- Aldrich, Steinheim, Germany) was mixed with 10% (w/v) KOH at a ratio of 1:1, applied to the sample, and incubated for 15 min at room temperature before inspection by fluorescence microscopy at 350 nm and 25% laser light transmission (Nikon Eclipse 600, UV- 2A filter, Düsseldorf, Germany).

    Software:

    Article Title: Confrontations of the Pathogenic Fungus Colletotrichum graminicola With a Biocontrol Bacterium or a Ubiquitous Fungus Trigger Synthesis of Secondary Metabolites With Lead Structures of Synthetic Fungicides.
    Article Snippet: Differential interference contrast (DIC) and fluorescence microscopy were performed using a Nikon Eclipse 600 microscope (Nikon, Düsseldorf, Germany). .. Digital images were taken with a Nikon microscope camera DS- Ri2, and image processing was performed with NIS- Elements imaging software (Nikon, Düsseldorf, Germany). .. For straining of fungal cell walls, Calcofluor White- M2R (CFW; Sigma- Aldrich, Steinheim, Germany) was mixed with 10% (w/v) KOH at a ratio of 1:1, applied to the sample, and incubated for 15 min at room temperature before inspection by fluorescence microscopy at 350 nm and 25% laser light transmission (Nikon Eclipse 600, UV- 2A filter, Düsseldorf, Germany).



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    Image Search Results


    cLTP-enhanced recycling facilitates TrkB-FL translocation into postsynaptic densities. A, Hippocampal neurons (18 DIV) were transfected with GFP and treated with various agents as indicated. Endogenous TrkB-FL stained by the Trk (C-14) antibody that recognizes the C terminus of Trk (catalog# sc-11; Santa Cruz Biotechnology) was labeled red. Arrowheads and arrows denote protrusions with and without TrkB in the spine head, respectively. Scale bars, 1 μm. B, Three types of TrkB-FL distribution in spines. Scale bars, 2 μm. C, Proportions of spines containing TrkB-FL in the indicated locations. Graphs represent means ± SEM (n = 116, 169, and 135 spines analyzed from 8, 8, and 10 neurons, respectively, *p < 0.05 relative to no BDNF control of each group, #p < 0.05, χ2 test. D, Coimmunofluorescence labeling of recycled TrkB and PSD-95 in neurons (9 DIV) transfected with pcDNA3.1 or pCAGIG-GFP-Rab11S25N. Hippocampal neurons were stained for recycled TrkB (green) and PSD-95 (red) with (left) or without (right) glycine stimulation. Blue indicates neurons expressing pcAGIG-GFP-Rab11S25N. Colocalization is indicated by white arrows. Scale bars, 10 μm. E, Quantification analysis of the colocalization of recycled TrkB-FL or TrkB.T1 with PSD-95 in D. Graphs represent means ± SEM (n ≥ 30 cells for each condition per experiment, ***p < 0.001 relative to its baseline, #p < 0.05, Student's t test). F, Quantification analysis of the clusters of PSD95. Images were taken using a 100× objective and two-dimensional deconvolution software (MetaMorph) was used.

    Journal: The Journal of Neuroscience

    Article Title: BDNF-Dependent Recycling Facilitates TrkB Translocation to Postsynaptic Density during LTP via a Rab11-Dependent Pathway

    doi: 10.1523/JNEUROSCI.3256-12.2013

    Figure Lengend Snippet: cLTP-enhanced recycling facilitates TrkB-FL translocation into postsynaptic densities. A, Hippocampal neurons (18 DIV) were transfected with GFP and treated with various agents as indicated. Endogenous TrkB-FL stained by the Trk (C-14) antibody that recognizes the C terminus of Trk (catalog# sc-11; Santa Cruz Biotechnology) was labeled red. Arrowheads and arrows denote protrusions with and without TrkB in the spine head, respectively. Scale bars, 1 μm. B, Three types of TrkB-FL distribution in spines. Scale bars, 2 μm. C, Proportions of spines containing TrkB-FL in the indicated locations. Graphs represent means ± SEM (n = 116, 169, and 135 spines analyzed from 8, 8, and 10 neurons, respectively, *p < 0.05 relative to no BDNF control of each group, #p < 0.05, χ2 test. D, Coimmunofluorescence labeling of recycled TrkB and PSD-95 in neurons (9 DIV) transfected with pcDNA3.1 or pCAGIG-GFP-Rab11S25N. Hippocampal neurons were stained for recycled TrkB (green) and PSD-95 (red) with (left) or without (right) glycine stimulation. Blue indicates neurons expressing pcAGIG-GFP-Rab11S25N. Colocalization is indicated by white arrows. Scale bars, 10 μm. E, Quantification analysis of the colocalization of recycled TrkB-FL or TrkB.T1 with PSD-95 in D. Graphs represent means ± SEM (n ≥ 30 cells for each condition per experiment, ***p < 0.001 relative to its baseline, #p < 0.05, Student's t test). F, Quantification analysis of the clusters of PSD95. Images were taken using a 100× objective and two-dimensional deconvolution software (MetaMorph) was used.

    Article Snippet: Images were taken using a 100× objective and two-dimensional deconvolution software (MetaMorph) was used.

    Techniques: Translocation Assay, Transfection, Staining, Labeling, Control, Expressing, Software